Výsledky vyhledávání - "N.D.L. George"

Who should manage primary retinal detachments?

Autor: N.D.L. George, Douglas K Newman, Anthony T. Moore, Brian D. M. Tom, Marie Comer, Keith R Martin

Publikováno v: Eye. 14:572-578

Purpose To determine whether the outcome of primary retinal reattachment surgery in a subregion is improved by surgery being performed in a specialist vitreoretinal unit (VRU). Methods A subregional, population-based, retrospective audit cycle of pri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef1182e559dc567b731f664d714b091
https://doi.org/10.1038/eye.2000.145

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[Untitled]

Autor: N.D.L. George, Anthony T. Moore, Dorothy Trump, K. Bradshaw

Publikováno v: Documenta Ophthalmologica. 98:153-173

Intensity-series rod and cone ERGs were recorded in 19 patients with XLRS and 26 control eyes. All patients were examined by one ophthalmologist and diagnosed on the basis of fundus appearance and evidence of the disease in other males in the same fa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2de31786d21f47043d93c06f5f284f79
https://doi.org/10.1023/a:1002432919073

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Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

Autor: Caraline L. Coats, André Hanauer, Ulrich Kellner, E.J.M. Schuurman, Niklas Dahl, Beate Niesler, N. Tijmes, Susannah M. Walpole, Ute Schulz, Anne Rantala, S.A. Gaythor, A.M. Bardelli, Eugenio Montini, G.J.B. van Ommen, Christina L. McHenry, C. Oudet, A. Blankenagel, J.E. Richards, H.G. Brunner, Andrea Ballabio, E. van de Vosse, P.T.V.M. de Jong, J.T. Dendunnen, Carmen Ayuso, E.L. Bingham, L Huopaniemi, Gudrun A. Rappold, K. Ruether, Thomas Rosenberg, Vera M. Kalscheuer, V. Ventruto, Paul A. Sieving, Arthur A.B. Bergen, Hanno J. Bolz, Ulrike Orth, T. Kraayenbrink, D. Pimenides, M.J. van Schooneveld, Andreas Gal, Alan F. Wright, N.D.L. George, Grazia Andolfi, F.J. Diaz, Brunella Franco, H.H. Ropers, Silke Feil, John R.W. Yates, Wolfgang Berger, Tiina Alitalo, Alfred J. L. G. Pinckers, A. dela Chapelle, U.T. Moore, J. Kaplan, Dorothy Trump, Steffen Lenzner, Pierre Bitoun, A. Nicolaou, K.T. Hiriyana, Hemant Pawar, T. Darga, J.B. ten Brink

Publikováno v: Human molecular genetics, 7(7), 1185-1192. Oxford University Press
Human Molecular Genetics, 7(7), 1185-1192. Oxford University Press

X-linked retinoschisis (XLRS) is the most common cause of juvenile macular degeneration in males, resulting in vision loss early in life. The gene involved in XLRS was identified recently. It encodes a protein with a disoidin domain, suggested to be

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f0fd99a148b526ec431d89cab82bed
https://pure.amc.nl/en/publications/functional-implications-of-the-spectrum-of-mutations-found-in-234-cases-with-xlinked-juvenile-retinoschisis-xlrs(1e0da310-81f1-413d-914c-b73a21b1a089).html

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